| Year |
Citation |
Score |
| 2022 |
Yang L, Xie F, Liu C, Zhao J, Hu T, Wu J, Zhao X, Wang S. Germline Variants in 32 Cancer-Related Genes among 700 Chinese Breast Cancer Patients by Next-Generation Sequencing: A Clinic-Based, Observational Study. International Journal of Molecular Sciences. 23. PMID 36232564 DOI: 10.3390/ijms231911266 |
0.359 |
|
| 2022 |
Hu T, Li J, Long M, Wu J, Zhang Z, Xie F, Zhao J, Yang H, Song Q, Lian S, Shi J, Guo X, Yuan D, Lang D, Yu G, et al. Detection of Structural Variations and Fusion Genes in Breast Cancer Samples Using Third-Generation Sequencing. Frontiers in Cell and Developmental Biology. 10: 854640. PMID 35493102 DOI: 10.3389/fcell.2022.854640 |
0.387 |
|
| 2022 |
Wu J, Liu H, Hu T, Wang S. Gene expression trend changes in breast cancer populations over two decades: insights from The Cancer Genome Atlas database. Hereditas. 159: 18. PMID 35317849 DOI: 10.1186/s41065-022-00230-3 |
0.304 |
|
| 2020 |
Ullah A, Long X, Mat WK, Hu T, Khan MI, Hui L, Zhang X, Sun P, Gao M, Wang J, Wang H, Li X, Sun W, Qiao M, Xue H. Highly Recurrent Copy Number Variations in Associated With Schizophrenia and Premenstrual Dysphoric Disorder. Frontiers in Psychiatry. 11: 572. PMID 32695026 DOI: 10.3389/Fpsyt.2020.00572 |
0.444 |
|
| 2020 |
Wu Z, Long X, Tsang SY, Hu T, Yang JF, Mat WK, Wang H, Xue H. Genomic subtyping of liver cancers with prognostic application. Bmc Cancer. 20: 84. PMID 32005109 DOI: 10.1186/S12885-020-6546-8 |
0.543 |
|
| 2019 |
Hu T, Chen S, Ullah A, Xue H. AluScanCNV2: An R package for copy number variation calling and cancer risk prediction with next-generation sequencing data. Genes & Diseases. 6: 43-46. PMID 30906832 DOI: 10.1016/J.Gendis.2018.09.001 |
0.525 |
|
| 2018 |
Hu T, Kumar Y, Shazia I, Duan SJ, Li Y, Chen L, Chen JF, Yin R, Kwong A, Leung GK, Mat WK, Wu Z, Long X, Chan CH, Chen S, et al. Forward and reverse mutations in stages of cancer development. Human Genomics. 12: 40. PMID 30134973 DOI: 10.1186/S40246-018-0170-6 |
0.502 |
|
| 2016 |
Wong JT, Ng SK, Mat WK, Hu T, Xue H. Coevolution Theory of the Genetic Code at Age Forty: Pathway to Translation and Synthetic Life. Life (Basel, Switzerland). 6. PMID 26999216 DOI: 10.3390/Life6010012 |
0.401 |
|
| 2016 |
Ng SK, Hu T, Long X, Chan CH, Tsang SY, Xue H. Feature co-localization landscape of the human genome. Scientific Reports. 6: 20650. PMID 26854351 DOI: 10.1038/Srep20650 |
0.494 |
|
| 2015 |
Kim YS, Yang M, Mat WK, Tsang SY, Su Z, Jiang X, Ng SK, Liu S, Hu T, Pun F, Liao Y, Tang J, Chen X, Hao W, Xue H. GABRB2 Haplotype Association with Heroin Dependence in Chinese Population. Plos One. 10: e0142049. PMID 26561861 DOI: 10.1371/Journal.Pone.0142049 |
0.438 |
|
| 2015 |
Kumar Y, Yang J, Hu T, Chen L, Xu Z, Xu L, Hu XX, Tang G, Wang JM, Li Y, Poon WS, Wan W, Zhang L, Mat WK, Pun FW, et al. Massive interstitial copy-neutral loss-of-heterozygosity as evidence for cancer being a disease of the DNA-damage response. Bmc Medical Genomics. 8: 42. PMID 26208496 DOI: 10.1186/S12920-015-0104-2 |
0.564 |
|
| Show low-probability matches. |